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Natural Selection in the Tropical Treehopper Alchisme Grossa (Hemiptera: Membracidae) on Two Sympatric Host- Plants

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Natural Selection in the Tropical Treehopper Alchisme Grossa (Hemiptera: Membracidae) on Two Sympatric Host- Plants Natural selection in the tropical treehopper Alchisme grossa (Hemiptera: Membracidae) on two sympatric host- plants Daniel Torrico-Bazoberry, Carlos F. Pinto, Luis Flores-Prado, Francisco E. Fontúrbel & Hermann M. Niemeyer Arthropod-Plant Interactions An international journal devoted to studies on interactions of insects, mites, and other arthropods with plants ISSN 1872-8855 Volume 10 Number 3 Arthropod-Plant Interactions (2016) 10:229-235 DOI 10.1007/s11829-016-9427-y 1 23 Your article is protected by copyright and all rights are held exclusively by Springer Science +Business Media Dordrecht. This e-offprint is for personal use only and shall not be self- archived in electronic repositories. If you wish to self-archive your article, please use the accepted manuscript version for posting on your own website. You may further deposit the accepted manuscript version in any repository, provided it is only made publicly available 12 months after official publication or later and provided acknowledgement is given to the original source of publication and a link is inserted to the published article on Springer's website. The link must be accompanied by the following text: "The final publication is available at link.springer.com”. 1 23 Author's personal copy Arthropod-Plant Interactions (2016) 10:229–235 DOI 10.1007/s11829-016-9427-y ORIGINAL PAPER Natural selection in the tropical treehopper Alchisme grossa (Hemiptera: Membracidae) on two sympatric host-plants 1,2 1,2,3 4 Daniel Torrico-Bazoberry • Carlos F. Pinto • Luis Flores-Prado • 5 1 Francisco E. Fontu´rbel • Hermann M. Niemeyer Received: 15 December 2014 / Accepted: 24 March 2016 / Published online: 8 April 2016 Ó Springer Science+Business Media Dordrecht 2016 Abstract The pronotum is the most distinctive and rep- linear selection acting upon pronotum length considering resentative structure in treehoppers. Although several the number of eggs and the late survival fitness proxies and functions have been proposed for this structure, its positive linear selection acting on the distance between the involvement in fitness has not been formally evaluated. suprahumeral horns considering the early survival proxy on Given the high degree of maternal investment exhibited by females ovipositing on both host-plants. These results the subsocial membracid Alchisme grossa (Hoplophorion- highlight the importance of the pronotum in treehoppers ini), the pronotum has been suggested as a shield for off- females’ fitness and suggest that maternal care appears to spring protection. We performed selection gradient have a greater importance in the way that natural selection analyses on A. grossa in order to evaluate how natural is operating than the host-plant where oviposition occurs. selection is acting upon two traits associated with this structure considering three different fitness proxies: (1) Keywords Bolivia Á Phenotypic selection Á Pronotum Á number of eggs, (2) the ratio between the number of first- Selection gradients Á Yungas stage nymphs and the number of eggs (early survival), and (3) the number of third-stage nymphs (late survival). Since A. grossa feeds, oviposits and mates on two alternative Introduction host-plants (Brugmansia suaveolens and Solanum ursinum, both Solanaceae), we also evaluated and compared selec- Parental care in insects, defined as behavioral displays of tion gradients between these host-plants. We found positive one or both parents during the post-ovipositional phase that enhance survival, growth and development of the offspring (Tallamy and Wood 1986), is widely distributed among Handling Editor: Heikki Hokkanen. several species, being present in at least 47 families & Carlos F. Pinto belonging to 13 orders (Choe and Crespi 1997; Lin 2006; [email protected] Trumbo 2012). Parental care is frequently performed by females (i.e., maternal care) and shows a variable duration 1 ´ ´ Laboratorio de Quımica Ecologica, Facultad de Ciencias, in relation to the life cycle stages of the offspring under Universidad de Chile, Las Palmeras 3425, Santiago, Chile protection (Godoy et al. 2006). Treehoppers (Hemiptera: 2 ´ ´ Laboratorio de Ecologıa Quımica, Facultad de Ciencias y Membracidae) are one of the best-known taxonomic groups Tecnologı´a, Universidad Mayor de San Simo´n, Parque La Torre # 1720, Cochabamba, Bolivia in which parental care consists mainly in the permanence and vigilance of the mother around its offspring, thus 3 Universidad Mayor Real y Pontificia de San Francisco Xavier de Chuquisaca, Estudiantes # 97, Sucre, Bolivia providing active protection against predators (Lin et al. 2004; Godoy et al. 2006; Lin 2006). 4 Instituto de Entomologı´a, Universidad Metropolitana de Ciencias de la Educacio´n, Av. Jose´ Pedro Alessandri 774, In some treehopper species, maternal care shows a short Santiago, Chile duration and the task is then transferred to hymenopteran 5 Laboratorio de Ecologı´a Evolutiva, Facultad de Ciencias, insects (mostly ants). These insects defend and take care of Universidad de Chile, Las Palmeras 3425, Santiago, Chile the progeny (Bristow 1983; Godoy et al. 2006) and in 123 Author's personal copy 230 D. Torrico-Bazoberry et al. return receive a sweet substance (known as honeydew) plants. Taking into account that the pronotum has been from nymphs (Del-Claro and Oliveira 1996, 1999), thus suggested as a shield-like structure (McKamey and Deitz establishing a mutualistic interaction (Wood 1984; Godoy 1996; Camacho et al. 2014), which serves as protection et al. 2006). Mutualism with ants and other hymenopterans against the attack of the most common predators of this is totally absent in treehoppers of the tribe Hoplophorion- species in this location (Reduviidae and Coccinellidae ini, and maternal care relies exclusively on females and insects), and that females use it to deter predator attacks extends until the progeny reaches the adult stage (McKa- against its offspring through body twisting (Torrico-Ba- mey and Deitz 1996; Lin et al. 2004; Torrico-Bazoberry zoberry et al. 2014), three traits: pronotum length, distance et al. 2014). Species of this tribe show the highest degree of between the suprahumeral horns, and the distance between maternal care among treehoppers (McKamey and Deitz the tip of the dorsal process and the right suprahumeral 1996), in terms of behavioral (Wood 1974, 1976; Cocroft horn were examined under a selection gradient analyses. 2002; Lin 2006), communicational (Nault et al. 1974; Cocroft 1996, 1999a, b; Ramaswamy and Cocroft 2009) and morphological (Crea˜o-Duarte and Sakakibara 1997; Materials and methods Wood 1993; Lin 2006; Camacho et al. 2014) adaptations that allow them to effectively defend their offspring. Study area and data collection Among those morphological adaptations, the pronotum has been associated with roles such as sensorial, crypsis Data were collected during two consecutive rainy seasons: and protection against vertebrate (Poulton 1903; Wood and December 2012–March 2013 and December 2013–Febru- Morris 1974; Wood 1975, 1976, 1977, 1993) and inverte- ary 2014 at Incachaca (Cochabamba, Bolivia, 17°130S– brate predators and parasitoids (Boulard 1983; Wood 1993; 65°490W; 2450 m.a.s.l.), within the Yungas biogeographi- Lin 2006; Camacho et al. 2014). Furthermore, female cal region. Plants of B. suaveolens and S. ursinum that treehoppers have generally bigger pronotum than males hosted reproductive females associated with egg masses (Crea˜o-Duarte and Sakakibara 1997; Godoy et al. 2006); (from now on called families) were identified. A tag was given the occurrence of maternal care, this suggests that the attached to the petiole of the leaf where each family was pronotum is important for offspring protection and/or egg found; additionally, the pronotum of each female was mass covering (Camacho et al. 2014). Although the marked on the right side with a permanent marker. Pre- pronotum of treehoppers seems to represent a morpholog- liminary observations carried out in A. grossa females had ical adaptation, the way that natural selection operates on shown that there was no significant difference in mortality this structure in relation with maternal care has not yet between marked and unmarked females (v2 = 0.075; been formally evaluated. d.f. = 1; p = 0.743), based on a 3-month observation Alchisme grossa (Hoplophorionini) is a widely dis- period. tributed Neotropical treehopper (McKamey and Deitz 1996; Lin et al. 2004), which is characterized by exhibiting Phenotypic traits maternal care until offspring development is completed (Camacho et al. 2014; Torrico-Bazoberry et al. 2014). One hundred and eighty-one families were marked during According to previous observations performed within a site two rainy seasons: 120 during the 2012–2013 season (69 in the Yungas biogeographical region, the insect develops distributed on 30 plants of B. suaveolens and 51 on 35 its life cycle using two species of alternative host-plants: plants of S. ursinum) and 61 families during the 2013–2014 Brugmansia suaveolens and Solanum ursinum (both Sola- season (31 on 9 plants of B. suaveolens and 30 on 17 plants naceae) (Torrico-Bazoberry et al. 2014). Additionally, the of S. ursinum). All marked families were monitored every close dependence of A. grossa on its two alternative host- 5 days (between 11:00 and 14:00 h) until nymphs disag- plants (as feeding, mating and oviposition sites) constitute gregated from their original families. In order to investigate a scenario where the local conditions (biotic and abiotic) of how natural selection operates on characteristics of the each host-plant may exert differential selective pressures pronotum of each mother, the following traits were mea- on the insects, as has been suggested and reported for some sured using a digital caliper (0.01 mm precision): (1) treehoppers and other insects (Keese and Wood 1991; pronotum length (PL), (2) distance between suprahumeral Wood et al. 1999; Cocroft et al. 2008, 2010; Ruiz-Montoya horns (DSH), and (3) distance between the tip of the dorsal and Nu´n˜ez-Farfa´n 2009; Flores-Prado et al. 2014). Hence, process and the right suprahumeral horn (DDPSH) (Godoy using A. grossa as a model organism, we evaluated and et al.
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